4.6 Article

Importance of catecholamine signaling in the development of platelet exhaustion after traumatic injury

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 20, 期 9, 页码 2109-2118

出版社

WILEY
DOI: 10.1111/jth.15763

关键词

blood coagulation disorders; catecholamines; platelet activation; platelet aggregation; platelets; trauma

资金

  1. NIH [1K23GM130892-01, R01-HL149670]
  2. DoD [W911QY-15-C-0044]
  3. [UL1 TR001872]

向作者/读者索取更多资源

This study aimed to determine the relationship between catecholamines and platelet-dependent hemostasis after injury, as well as to model catecholamine-induced functional platelet exhaustion in healthy donor platelets. The study found that epinephrine and norepinephrine were associated with impaired platelet aggregation in trauma patients. In healthy donors, short incubation with epinephrine enhanced platelet aggregation, platelet adhesion, and glycoprotein IIb/IIIa activation, while longer incubation resulted in decreased platelet adhesion, aggregation, and surface expression of glycoprotein IIb/IIIa.
Background Impaired ex vivo platelet aggregation is common in trauma patients. The mechanisms driving these impairments remain incompletely understood, but functional platelet exhaustion due to excessive in vivo activation is implicated. Given platelet adrenoreceptors and known catecholamine surges after injury, impaired ex vivo platelet aggregation in trauma patients may be linked to catecholamine-induced functional platelet exhaustion. Objective To determine the relationship of catecholamines with platelet-dependent hemostasis after injury and to model catecholamine-induced functional platelet exhaustion in healthy donor platelets. Patients/Methods Whole blood was collected from 67 trauma patients as part of a prospective cohort study. Platelet aggregometry and rotational thromboelastometry were performed, and plasma epinephrine (EPI) and norepinephrine (NE) concentrations were measured. The effect of catecholamines on healthy donor platelets was examined in a microfluidic model, with platelet aggregometry, and by flow cytometry examining surface markers of platelet activation. Results In trauma patients, EPI and NE were associated with impaired platelet aggregation (both p < 0.05), and EPI was additionally associated with decreased viscoelastic clot strength, increased fibrinolysis, and mortality (all p < 0.05). In healthy donors, short duration incubation with EPI enhanced platelet aggregation, platelet adhesion under flow, and increased glycoprotein IIb/IIIa activation, while weaker effects were observed with NE. Compared with short incubation, longer incubation with EPI resulted in decreased platelet adhesion, platelet aggregation, and surface expression of glycoprotein IIb/IIIa. Conclusions These findings suggest sympathoadrenal activation in trauma patients contributes to impaired ex vivo platelet aggregation, which mechanistically may be explained by a functionally exhausted platelet phenotype under prolonged exposure to high plasma catecholamine levels.

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